Canonical Allele Identifier: CA931721160

Gene: ABCC2

Linked Data

• dbSNP Id: rs2038212313
• gnomAD v3: 10-99811485-A-T
• gnomAD v4: 10-99811485-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99811485A>T , CM000672.2:g.99811485A>T	GRCh38
NC_000010.10:g.101571242A>T , CM000672.1:g.101571242A>T	GRCh37
NC_000010.9:g.101561232A>T	NCBI36
NG_011798.1:g.33780A>T
NG_011798.2:g.33888A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.1901-51A>T MANE Select	ENSP00000497274.1:n.1901-51A>T
ENST00000370449.8:c.1901-51A>T	ENSP00000359478.4:n.1901-51A>T
NM_000392.4:c.1901-51A>T	NP_000383.1:n.1901-51A>T
XM_006717630.2:c.1205-51A>T	XP_006717693.1:n.1205-51A>T
XM_006717631.2:c.1901-51A>T	XP_006717694.1:n.1901-51A>T
XM_011539291.1:c.1901-51A>T	XP_011537593.1:n.1901-51A>T
XR_945604.1:n.2090-51A>T
XR_945605.1:n.2092-51A>T
NM_000392.5:c.1901-51A>T MANE Select	NP_000383.2:n.1901-51A>T
XM_006717630.3:c.1205-51A>T	XP_006717693.1:n.1205-51A>T
XM_006717631.4:c.1901-51A>T	XP_006717694.1:n.1901-51A>T
XM_011539291.3:c.1901-51A>T	XP_011537593.1:n.1901-51A>T
XM_017015675.2:c.1901-51A>T	XP_016871164.1:n.1901-51A>T
XR_945604.3:n.2144-51A>T
XR_945605.3:n.2144-51A>T