Canonical Allele Identifier: CA2581047037
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112166831C>T , CM000673.2:g.112166831C>T GRCh38
NC_000011.9:g.112037554C>T , CM000673.1:g.112037554C>T GRCh37
NC_000011.8:g.111542764C>T NCBI36
NG_028143.1:g.2287G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000525987.5:n.320-3588C>T
ENST00000531744.5:c.315-3588C>T ENSP00000456957.1:n.315-3588C>T
ENST00000532699.1:c.315-3588C>T ENSP00000456434.1:n.315-3588C>T