Canonical Allele Identifier: CA2518365981
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112164748C>T , CM000673.2:g.112164748C>T GRCh38
NC_000011.9:g.112035471C>T , CM000673.1:g.112035471C>T GRCh37
NC_000011.8:g.111540681C>T NCBI36
NG_028143.1:g.4370G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000525987.5:n.320-5671C>T
ENST00000531744.5:c.315-5671C>T ENSP00000456957.1:n.315-5671C>T
ENST00000532699.1:c.315-5671C>T ENSP00000456434.1:n.315-5671C>T