Canonical Allele Identifier: CA5643856
Gene: ABCC2 HGNC NCBI

Linked Data

dbSNP Id: rs779633376

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99836257A>T , CM000672.2:g.99836257A>T GRCh38
NC_000010.10:g.101596014A>T , CM000672.1:g.101596014A>T GRCh37
NC_000010.9:g.101586004A>T NCBI36
NG_011798.1:g.58552A>T
NG_011798.2:g.58660A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3581A>T MANE Select ENSP00000497274.1:p.Gln1194Leu
ENST00000370449.8:c.3581A>T ENSP00000359478.4:p.Gln1194Leu
NM_000392.4:c.3581A>T NP_000383.1:p.Gln1194Leu
XM_006717630.2:c.2885A>T XP_006717693.1:p.Gln962Leu
XR_945604.1:n.3770A>T
XR_945605.1:n.3772A>T
NM_000392.5:c.3581A>T MANE Select NP_000383.2:p.Gln1194Leu
XM_006717630.3:c.2885A>T XP_006717693.1:p.Gln962Leu
XR_945604.3:n.3824A>T
XR_945605.3:n.3824A>T