Canonical Allele Identifier: CA2610262439
Gene:

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762618A>G , CM000672.2:g.94762618A>G GRCh38
NC_000010.10:g.96522375A>G , CM000672.1:g.96522375A>G GRCh37
NC_000010.9:g.96512365A>G NCBI36
NG_008384.2:g.4913A>G
NG_008384.3:g.4938A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000464755.1:c.932-12440A>G ENSP00000483243.1:n.932-12440A>G