Canonical Allele Identifier: CA278674975

Gene: ABCC6

Linked Data

• dbSNP Id: rs865962652
• gnomAD v4: 16-16150124-G-A
• MyVariant Identifiers: chr16:g.16243981G>A (hg19) ; chr16:g.16150124G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16150124G>A , CM000678.2:g.16150124G>A	GRCh38
NC_000016.9:g.16243981G>A , CM000678.1:g.16243981G>A	GRCh37
NC_000016.8:g.16151482G>A	NCBI36
NG_007558.2:g.78348C>T
NG_007558.3:g.78494C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*693C>T	ENSP00000483331.2:n.*693C>T
ENST00000205557.12:c.*9C>T MANE Select	ENSP00000205557.7:n.*9C>T
ENST00000640696.1:c.1335C>T	ENSP00000492197.1:n.1335C>T
ENST00000205557.11:c.*9C>T	ENSP00000205557.7:n.*9C>T
ENST00000576204.5:n.1384C>T
ENST00000622290.4:c.*1730C>T	ENSP00000483331.1:n.*1730C>T
NM_001171.5:c.*9C>T	NP_001162.4:n.*9C>T
XM_011522479.1:c.*9C>T	XP_011520781.1:n.*9C>T
XM_011522480.1:c.*9C>T	XP_011520782.1:n.*9C>T
XM_011522481.1:c.*9C>T	XP_011520783.1:n.*9C>T
XR_933134.1:n.538+5834G>A
NM_001351800.1:c.*9C>T	NP_001338729.1:n.*9C>T
NR_147784.1:n.4183C>T
XM_011522479.2:c.*9C>T	XP_011520781.1:n.*9C>T
XM_011522481.3:c.*9C>T	XP_011520783.1:n.*9C>T
XM_017023212.1:c.*9C>T	XP_016878701.1:n.*9C>T
XM_024450261.1:c.*9C>T	XP_024306029.1:n.*9C>T
NM_001171.6:c.*9C>T MANE Select	NP_001162.5:n.*9C>T