Canonical Allele Identifier: CA378124333

Gene: ABCC2

Linked Data

• dbSNP Id: rs2038817059
• MyVariant Identifiers: chr10:g.101595867C>T (hg19) ; chr10:g.99836110C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99836110C>T , CM000672.2:g.99836110C>T	GRCh38
NC_000010.10:g.101595867C>T , CM000672.1:g.101595867C>T	GRCh37
NC_000010.9:g.101585857C>T	NCBI36
NG_011798.1:g.58405C>T
NG_011798.2:g.58513C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3434C>T MANE Select	ENSP00000497274.1:p.Ser1145Phe
ENST00000370449.8:c.3434C>T	ENSP00000359478.4:p.Ser1145Phe
NM_000392.4:c.3434C>T	NP_000383.1:p.Ser1145Phe
XM_006717630.2:c.2738C>T	XP_006717693.1:p.Ser913Phe
XR_945604.1:n.3623C>T
XR_945605.1:n.3625C>T
NM_000392.5:c.3434C>T MANE Select	NP_000383.2:p.Ser1145Phe
XM_006717630.3:c.2738C>T	XP_006717693.1:p.Ser913Phe
XR_945604.3:n.3677C>T
XR_945605.3:n.3677C>T