Canonical Allele Identifier: CA2700222260
Gene:

Linked Data

dbSNP Id: rs2104511503

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.118079688A>C , CM000664.2:g.118079688A>C GRCh38
NC_000002.11:g.118837264A>C , CM000664.1:g.118837264A>C GRCh37
NC_000002.10:g.118553734A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011512305.1:c.697-2156T>G XP_011510607.1:n.697-2156T>G
XR_001739662.2:n.138+8563T>G