Canonical Allele Identifier: CA2714350195
Gene:

Linked Data

dbSNP Id: rs2128585653

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30897609T>C , CM000669.2:g.30897609T>C GRCh38
NC_000007.13:g.30937224T>C , CM000669.1:g.30937224T>C GRCh37
NC_000007.12:g.30903749T>C NCBI36
NG_007475.2:g.49216T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000509504.2:c.622-14384T>C