Canonical Allele Identifier: CA837538775
Gene:

Linked Data

dbSNP Id: rs1173145937

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30897574A>G , CM000669.2:g.30897574A>G GRCh38
NC_000007.13:g.30937189A>G , CM000669.1:g.30937189A>G GRCh37
NC_000007.12:g.30903714A>G NCBI36
NG_007475.2:g.49181A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.622-14419A>G