Canonical Allele Identifier: CA471128871

Gene: ABCC2

Linked Data

• MyVariant Identifiers: chr10:g.101571300C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99811543C>T , CM000672.2:g.99811543C>T	GRCh38
NC_000010.10:g.101571300C>T , CM000672.1:g.101571300C>T	GRCh37
NC_000010.9:g.101561290C>T	NCBI36
NG_011798.1:g.33838C>T
NG_011798.2:g.33946C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.1908C>T MANE Select	ENSP00000497274.1:p.Ala636=
ENST00000370449.8:c.1908C>T	ENSP00000359478.4:p.Ala636=
NM_000392.4:c.1908C>T	NP_000383.1:p.Ala636=
XM_006717630.2:c.1212C>T	XP_006717693.1:p.Ala404=
XM_006717631.2:c.1908C>T	XP_006717694.1:p.Ala636=
XM_011539291.1:c.1908C>T	XP_011537593.1:p.Ala636=
XR_945604.1:n.2097C>T
XR_945605.1:n.2099C>T
NM_000392.5:c.1908C>T MANE Select	NP_000383.2:p.Ala636=
XM_006717630.3:c.1212C>T	XP_006717693.1:p.Ala404=
XM_006717631.4:c.1908C>T	XP_006717694.1:p.Ala636=
XM_011539291.3:c.1908C>T	XP_011537593.1:p.Ala636=
XM_017015675.2:c.1908C>T	XP_016871164.1:p.Ala636=
XR_945604.3:n.2151C>T
XR_945605.3:n.2151C>T