Canonical Allele Identifier: CA394876232

Gene: ABCC6

Linked Data

• gnomAD v4: 16-16155019-C-A
• MyVariant Identifiers: chr16:g.16248876C>A (hg19) ; chr16:g.16155019C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16155019C>A , CM000678.2:g.16155019C>A	GRCh38
NC_000016.9:g.16248876C>A , CM000678.1:g.16248876C>A	GRCh37
NC_000016.8:g.16156377C>A	NCBI36
NG_007558.2:g.73453G>T
NG_007558.3:g.73599G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000576204.6:n.758G>T
ENST00000622290.5:c.*67G>T	ENSP00000483331.2:n.*67G>T
ENST00000205557.12:c.3895G>T MANE Select	ENSP00000205557.7:p.Gly1299Cys
ENST00000640696.1:c.709G>T	ENSP00000492197.1:p.Gly237Cys
ENST00000205557.11:c.3895G>T	ENSP00000205557.7:p.Gly1299Cys
ENST00000456970.6:c.3520G>T	ENSP00000405002.2:n.3520G>T
ENST00000576204.5:n.758G>T
ENST00000622290.4:c.*1104G>T	ENSP00000483331.1:n.*1104G>T
NM_001171.5:c.3895G>T	NP_001162.4:p.Gly1299Cys
XM_011522479.1:c.3862G>T	XP_011520781.1:p.Gly1288Cys
XM_011522480.1:c.3553G>T	XP_011520782.1:p.Gly1185Cys
XM_011522481.1:c.3553G>T	XP_011520783.1:p.Gly1185Cys
XR_932836.1:n.4193G>T
XR_932837.1:n.3931G>T
XR_932838.1:n.3994G>T
XR_933134.1:n.539-4762C>A
NM_001351800.1:c.3553G>T	NP_001338729.1:p.Gly1185Cys
NR_147784.1:n.3557G>T
XM_011522479.2:c.3862G>T	XP_011520781.1:p.Gly1288Cys
XM_011522481.3:c.3553G>T	XP_011520783.1:p.Gly1185Cys
XM_017023212.1:c.3727G>T	XP_016878701.1:p.Gly1243Cys
XM_024450261.1:c.3931G>T	XP_024306029.1:p.Gly1311Cys
XR_932836.2:n.4139G>T
XR_932837.3:n.3876G>T
XR_932838.3:n.3939G>T
NM_001171.6:c.3895G>T MANE Select	NP_001162.5:p.Gly1299Cys