Canonical Allele Identifier: CA228571726
Gene:

Linked Data

dbSNP Id: rs921384696

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112164649C>T , CM000673.2:g.112164649C>T GRCh38
NC_000011.9:g.112035372C>T , CM000673.1:g.112035372C>T GRCh37
NC_000011.8:g.111540582C>T NCBI36
NG_028143.1:g.4469G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000525987.5:n.320-5770C>T
ENST00000531744.5:c.315-5770C>T ENSP00000456957.1:n.315-5770C>T
ENST00000532699.1:c.315-5770C>T ENSP00000456434.1:n.315-5770C>T