Canonical Allele Identifier: CA233489694

Gene: SLCO1C1

Linked Data

• dbSNP Id: rs753426462
• MyVariant Identifiers: chr12:g.20857412T>C (hg19) ; chr12:g.20704478T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.20704478T>C , CM000674.2:g.20704478T>C	GRCh38
NC_000012.11:g.20857412T>C , CM000674.1:g.20857412T>C	GRCh37
NC_000012.10:g.20748679T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266509.7:c.272-1471T>C MANE Select	ENSP00000266509.2:n.272-1471T>C
ENST00000266509.6:c.272-1471T>C	ENSP00000266509.2:n.272-1471T>C
ENST00000539415.5:c.129+4773T>C	ENSP00000437399.1:n.129+4773T>C
ENST00000540354.5:c.272-1471T>C	ENSP00000438665.1:n.272-1471T>C
ENST00000545102.1:c.-83-1471T>C	ENSP00000444527.1:n.-83-1471T>C
ENST00000545604.5:c.272-1471T>C	ENSP00000444149.1:n.272-1471T>C
NM_001145944.1:c.-83-1471T>C	NP_001139416.1:n.-83-1471T>C
NM_001145945.1:c.272-1471T>C	NP_001139417.1:n.272-1471T>C
NM_001145946.1:c.272-1471T>C	NP_001139418.1:n.272-1471T>C
NM_017435.4:c.272-1471T>C	NP_059131.1:n.272-1471T>C
XM_005253394.1:c.272-1471T>C	XP_005253451.1:n.272-1471T>C
XM_005253396.1:c.-83-1471T>C	XP_005253453.1:n.-83-1471T>C
XM_005253397.2:c.272-1471T>C	XP_005253454.1:n.272-1471T>C
XM_011520703.1:c.272-1471T>C	XP_011519005.1:n.272-1471T>C
XM_011520704.1:c.272-1471T>C	XP_011519006.1:n.272-1471T>C
XM_011520705.1:c.272-1471T>C	XP_011519007.1:n.272-1471T>C
XM_011520706.1:c.-83-1471T>C	XP_011519008.1:n.-83-1471T>C
XM_011520707.1:c.-83-1471T>C	XP_011519009.1:n.-83-1471T>C
XM_011520708.1:c.-83-1471T>C	XP_011519010.1:n.-83-1471T>C
XM_011520709.1:c.-83-1471T>C	XP_011519011.1:n.-83-1471T>C
XM_011520710.1:c.272-1471T>C	XP_011519012.1:n.272-1471T>C
XM_011520711.1:c.-282-1471T>C	XP_011519013.1:n.-282-1471T>C
XR_931308.1:n.627-1471T>C
XM_005253394.3:c.272-1471T>C	XP_005253451.1:n.272-1471T>C
XM_005253396.3:c.-83-1471T>C	XP_005253453.1:n.-83-1471T>C
XM_011520703.3:c.272-1471T>C	XP_011519005.1:n.272-1471T>C
XM_011520704.3:c.272-1471T>C	XP_011519006.1:n.272-1471T>C
XM_011520711.3:c.-282-1471T>C	XP_011519013.1:n.-282-1471T>C
XM_017019486.2:c.-83-1471T>C	XP_016874975.1:n.-83-1471T>C
XM_017019487.2:c.-83-1471T>C	XP_016874976.1:n.-83-1471T>C
XM_017019489.2:c.-439-1471T>C	XP_016874978.1:n.-439-1471T>C
XM_017019490.2:c.-403-1471T>C	XP_016874979.1:n.-403-1471T>C
XM_024449024.1:c.-83-1471T>C	XP_024304792.1:n.-83-1471T>C
XM_024449025.1:c.-83-1471T>C	XP_024304793.1:n.-83-1471T>C
XR_001748768.2:n.13685-1471T>C
XR_001748769.2:n.13685-1471T>C
XR_001748770.2:n.13685-1471T>C
XR_001748771.2:n.14182-1471T>C
NM_001145944.2:c.-83-1471T>C	NP_001139416.1:n.-83-1471T>C
NM_001145945.2:c.272-1471T>C	NP_001139417.1:n.272-1471T>C
NM_001145946.2:c.272-1471T>C	NP_001139418.1:n.272-1471T>C
NM_017435.5:c.272-1471T>C MANE Select	NP_059131.1:n.272-1471T>C