Canonical Allele Identifier: CA15866641

Gene: ABCC1

Linked Data

• dbSNP Id: rs212090
• gnomAD v2: 16-16236004-T-A
• gnomAD v3: 16-16142147-T-A
• gnomAD v4: 16-16142147-T-A
• MyVariant Identifiers: chr16:g.16236004T>A (hg19) ; chr16:g.16142147T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16142147T>A , CM000678.2:g.16142147T>A	GRCh38
NC_000016.9:g.16236004T>A , CM000678.1:g.16236004T>A	GRCh37
NC_000016.8:g.16143505T>A	NCBI36
NG_028268.1:g.197571T>A
NG_028268.2:g.197571T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000399408.7:c.*866T>A	ENSP00000382340.4:n.*866T>A
ENST00000399410.8:c.*866T>A MANE Select	ENSP00000382342.3:n.*866T>A
ENST00000572882.3:c.*866T>A	ENSP00000461615.2:n.*866T>A
ENST00000676806.1:n.2188T>A
ENST00000677164.1:c.*866T>A	ENSP00000502873.1:n.*866T>A
ENST00000678422.1:c.*2559T>A	ENSP00000503954.1:n.*2559T>A
ENST00000399408.6:c.*866T>A	ENSP00000382340.3:n.*866T>A
ENST00000399410.7:c.*866T>A	ENSP00000382342.3:n.*866T>A
NM_004996.3:c.*866T>A	NP_004987.2:n.*866T>A
XM_011522497.1:c.*866T>A	XP_011520799.1:n.*866T>A
XM_011522498.1:c.*866T>A	XP_011520800.1:n.*866T>A
XM_011522498.2:c.*866T>A	XP_011520800.1:n.*866T>A
XM_017023237.1:c.*866T>A	XP_016878726.1:n.*866T>A
XM_017023238.1:c.*866T>A	XP_016878727.1:n.*866T>A
XM_017023239.1:c.*866T>A	XP_016878728.1:n.*866T>A
XM_017023240.1:c.*866T>A	XP_016878729.1:n.*866T>A
XM_017023241.1:c.*866T>A	XP_016878730.1:n.*866T>A
XM_017023242.1:c.*866T>A	XP_016878731.1:n.*866T>A
NM_004996.4:c.*866T>A MANE Select	NP_004987.2:n.*866T>A