Canonical Allele Identifier: CA670630073
Gene: ABCC2 HGNC NCBI

Linked Data

dbSNP Id: rs1179545153

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99830226G>C , CM000672.2:g.99830226G>C GRCh38
NC_000010.10:g.101589983G>C , CM000672.1:g.101589983G>C GRCh37
NC_000010.9:g.101579973G>C NCBI36
NG_011798.1:g.52521G>C
NG_011798.2:g.52629G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.2621-81G>C MANE Select ENSP00000497274.1:n.2621-81G>C
ENST00000370449.8:c.2621-81G>C ENSP00000359478.4:n.2621-81G>C
NM_000392.4:c.2621-81G>C NP_000383.1:n.2621-81G>C
XM_006717630.2:c.1925-81G>C XP_006717693.1:n.1925-81G>C
XM_006717631.2:c.*48-81G>C XP_006717694.1:n.*48-81G>C
XM_011539291.1:c.2621-81G>C XP_011537593.1:n.2621-81G>C
XR_945604.1:n.2810-81G>C
XR_945605.1:n.2812-81G>C
NM_000392.5:c.2621-81G>C MANE Select NP_000383.2:n.2621-81G>C
XM_006717630.3:c.1925-81G>C XP_006717693.1:n.1925-81G>C
XM_006717631.4:c.*48-81G>C XP_006717694.1:n.*48-81G>C
XM_011539291.3:c.2621-81G>C XP_011537593.1:n.2621-81G>C
XR_945604.3:n.2864-81G>C
XR_945605.3:n.2864-81G>C