Canonical Allele Identifier: CA1929213323
Gene:

Linked Data

dbSNP Id: rs1848182469

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762506A>G , CM000672.2:g.94762506A>G GRCh38
NC_000010.10:g.96522263A>G , CM000672.1:g.96522263A>G GRCh37
NC_000010.9:g.96512253A>G NCBI36
NG_008384.2:g.4801A>G
NG_008384.3:g.4826A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000464755.1:c.932-12552A>G ENSP00000483243.1:n.932-12552A>G