Canonical Allele Identifier: CA394875721

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16248810C>G (hg19) ; chr16:g.16154953C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16154953C>G , CM000678.2:g.16154953C>G	GRCh38
NC_000016.9:g.16248810C>G , CM000678.1:g.16248810C>G	GRCh37
NC_000016.8:g.16156311C>G	NCBI36
NG_007558.2:g.73519G>C
NG_007558.3:g.73665G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000576204.6:n.824G>C
ENST00000622290.5:c.*133G>C	ENSP00000483331.2:n.*133G>C
ENST00000205557.12:c.3961G>C MANE Select	ENSP00000205557.7:p.Gly1321Arg
ENST00000640696.1:c.775G>C	ENSP00000492197.1:p.Gly259Arg
ENST00000205557.11:c.3961G>C	ENSP00000205557.7:p.Gly1321Arg
ENST00000456970.6:c.3586G>C	ENSP00000405002.2:n.3586G>C
ENST00000576204.5:n.824G>C
ENST00000622290.4:c.*1170G>C	ENSP00000483331.1:n.*1170G>C
NM_001171.5:c.3961G>C	NP_001162.4:p.Gly1321Arg
XM_011522479.1:c.3928G>C	XP_011520781.1:p.Gly1310Arg
XM_011522480.1:c.3619G>C	XP_011520782.1:p.Gly1207Arg
XM_011522481.1:c.3619G>C	XP_011520783.1:p.Gly1207Arg
XR_932836.1:n.4259G>C
XR_932837.1:n.3997G>C
XR_932838.1:n.4060G>C
XR_933134.1:n.539-4828C>G
NM_001351800.1:c.3619G>C	NP_001338729.1:p.Gly1207Arg
NR_147784.1:n.3623G>C
XM_011522479.2:c.3928G>C	XP_011520781.1:p.Gly1310Arg
XM_011522481.3:c.3619G>C	XP_011520783.1:p.Gly1207Arg
XM_017023212.1:c.3793G>C	XP_016878701.1:p.Gly1265Arg
XM_024450261.1:c.3997G>C	XP_024306029.1:p.Gly1333Arg
XR_932837.3:n.3942G>C
NM_001171.6:c.3961G>C MANE Select	NP_001162.5:p.Gly1321Arg