Canonical Allele Identifier: CA5643801

Gene: ABCC2

Linked Data

• dbSNP Id: rs759464360
• ExAC: 10:101595825 G / T
• gnomAD v2: 10-101595825-G-T
• gnomAD v4: 10-99836068-G-T
• MyVariant Identifiers: chr10:g.101595825G>T (hg19) ; chr10:g.99836068G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99836068G>T , CM000672.2:g.99836068G>T	GRCh38
NC_000010.10:g.101595825G>T , CM000672.1:g.101595825G>T	GRCh37
NC_000010.9:g.101585815G>T	NCBI36
NG_011798.1:g.58363G>T
NG_011798.2:g.58471G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.3415-23G>T MANE Select	ENSP00000497274.1:n.3415-23G>T
ENST00000370449.8:c.3415-23G>T	ENSP00000359478.4:n.3415-23G>T
NM_000392.4:c.3415-23G>T	NP_000383.1:n.3415-23G>T
XM_006717630.2:c.2719-23G>T	XP_006717693.1:n.2719-23G>T
XR_945604.1:n.3604-23G>T
XR_945605.1:n.3606-23G>T
NM_000392.5:c.3415-23G>T MANE Select	NP_000383.2:n.3415-23G>T
XM_006717630.3:c.2719-23G>T	XP_006717693.1:n.2719-23G>T
XR_945604.3:n.3658-23G>T
XR_945605.3:n.3658-23G>T