Canonical Allele Identifier: CA2610497669

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99844209-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844209A>C , CM000672.2:g.99844209A>C	GRCh38
NC_000010.10:g.101603966A>C , CM000672.1:g.101603966A>C	GRCh37
NC_000010.9:g.101593956A>C	NCBI36
NG_011798.1:g.66504A>C
NG_011798.2:g.66612A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3844-113A>C MANE Select	ENSP00000497274.1:n.3844-113A>C
ENST00000649459.1:n.192-113A>C
ENST00000370449.8:c.3844-113A>C	ENSP00000359478.4:n.3844-113A>C
NM_000392.4:c.3844-113A>C	NP_000383.1:n.3844-113A>C
XM_006717630.2:c.3148-113A>C	XP_006717693.1:n.3148-113A>C
XR_945604.1:n.4033-113A>C
XR_945605.1:n.3908-113A>C
NM_000392.5:c.3844-113A>C MANE Select	NP_000383.2:n.3844-113A>C
XM_006717630.3:c.3148-113A>C	XP_006717693.1:n.3148-113A>C
XR_945604.3:n.4087-113A>C
XR_945605.3:n.3960-113A>C