Canonical Allele Identifier: CA394885122

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16263708C>G (hg19) ; chr16:g.16169851C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16169851C>G , CM000678.2:g.16169851C>G	GRCh38
NC_000016.9:g.16263708C>G , CM000678.1:g.16263708C>G	GRCh37
NC_000016.8:g.16171209C>G	NCBI36
NG_007558.2:g.58621G>C
NG_007558.3:g.58767G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.2790G>C	ENSP00000483331.2:p.Val930=
ENST00000205557.12:c.2790G>C MANE Select	ENSP00000205557.7:p.Val930=
ENST00000205557.11:c.2790G>C	ENSP00000205557.7:p.Val930=
ENST00000456970.6:c.2615G>C	ENSP00000405002.2:p.Ter872Ser
ENST00000622290.4:c.2615G>C	ENSP00000483331.1:p.Ter872Ser
NM_001171.5:c.2790G>C	NP_001162.4:p.Val930=
XM_011522479.1:c.2757G>C	XP_011520781.1:p.Val919=
XM_011522480.1:c.2448G>C	XP_011520782.1:p.Val816=
XM_011522481.1:c.2448G>C	XP_011520783.1:p.Val816=
XR_932836.1:n.3025G>C
XR_932837.1:n.3026G>C
XR_932838.1:n.3026G>C
NM_001351800.1:c.2448G>C	NP_001338729.1:p.Val816=
NR_147784.1:n.2652G>C
XM_011522479.2:c.2757G>C	XP_011520781.1:p.Val919=
XM_011522481.3:c.2448G>C	XP_011520783.1:p.Val816=
XM_017023212.1:c.2622G>C	XP_016878701.1:p.Val874=
XM_017023214.1:c.2790G>C	XP_016878703.1:p.Val930=
XM_024450261.1:c.2826G>C	XP_024306029.1:p.Val942=
XR_932836.2:n.2971G>C
XR_932837.3:n.2971G>C
XR_932838.3:n.2971G>C
NM_001171.6:c.2790G>C MANE Select	NP_001162.5:p.Val930=