Canonical Allele Identifier: CA278634977

Gene: ABCC1

Linked Data

• dbSNP Id: rs573039780
• MyVariant Identifiers: chr16:g.16173135G>A (hg19) ; chr16:g.16079278G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16079278G>A , CM000678.2:g.16079278G>A	GRCh38
NC_000016.9:g.16173135G>A , CM000678.1:g.16173135G>A	GRCh37
NC_000016.8:g.16080636G>A	NCBI36
NG_028268.1:g.134702G>A
NG_028268.2:g.134702G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399408.7:c.1989-74G>A	ENSP00000382340.4:n.1989-74G>A
ENST00000399410.8:c.1989-74G>A MANE Select	ENSP00000382342.3:n.1989-74G>A
ENST00000572882.3:c.1989-74G>A	ENSP00000461615.2:n.1989-74G>A
ENST00000677164.1:c.1863-74G>A	ENSP00000502873.1:n.1863-74G>A
ENST00000678422.1:c.1989-74G>A	ENSP00000503954.1:n.1989-74G>A
ENST00000399408.6:c.1011-74G>A	ENSP00000382340.3:n.1011-74G>A
ENST00000399410.7:c.1989-74G>A	ENSP00000382342.3:n.1989-74G>A
ENST00000572882.2:c.1684-74G>A
ENST00000575422.5:n.229-74G>A
NM_004996.3:c.1989-74G>A	NP_004987.2:n.1989-74G>A
XM_011522497.1:c.1965-74G>A	XP_011520799.1:n.1965-74G>A
XM_011522498.1:c.1896-74G>A	XP_011520800.1:n.1896-74G>A
XM_011522498.2:c.1896-74G>A	XP_011520800.1:n.1896-74G>A
XM_017023237.1:c.2043-74G>A	XP_016878726.1:n.2043-74G>A
XM_017023238.1:c.1917-74G>A	XP_016878727.1:n.1917-74G>A
XM_017023239.1:c.1905-74G>A	XP_016878728.1:n.1905-74G>A
XM_017023240.1:c.2043-74G>A	XP_016878729.1:n.2043-74G>A
XM_017023241.1:c.1779-74G>A	XP_016878730.1:n.1779-74G>A
XM_017023242.1:c.2043-74G>A	XP_016878731.1:n.2043-74G>A
XM_017023243.2:c.2043-74G>A	XP_016878732.1:n.2043-74G>A
NM_004996.4:c.1989-74G>A MANE Select	NP_004987.2:n.1989-74G>A