Canonical Allele Identifier: CA1283487436
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120331875A= , CM000664.2:g.120331875A= GRCh38
NC_000002.11:g.121089451A= , CM000664.1:g.121089451A= GRCh37
NC_000002.10:g.120805921A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011512307.1:c.141+3069A= XP_011510609.1:n.141+3069A=