Canonical Allele Identifier: CA1697889762
Gene:

Linked Data

dbSNP Id: rs1353798449

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30897593G>T , CM000669.2:g.30897593G>T GRCh38
NC_000007.13:g.30937208G>T , CM000669.1:g.30937208G>T GRCh37
NC_000007.12:g.30903733G>T NCBI36
NG_007475.2:g.49200G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.622-14400G>T