Canonical Allele Identifier: CA2751927281
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120331931A>G , CM000664.2:g.120331931A>G GRCh38
NC_000002.11:g.121089507A>G , CM000664.1:g.121089507A>G GRCh37
NC_000002.10:g.120805977A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011512307.1:c.141+3125A>G XP_011510609.1:n.141+3125A>G