Canonical Allele Identifier: CA1283487438
Gene:

Linked Data

dbSNP Id: rs1690910063

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120331876G>C , CM000664.2:g.120331876G>C GRCh38
NC_000002.11:g.121089452G>C , CM000664.1:g.121089452G>C GRCh37
NC_000002.10:g.120805922G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011512307.1:c.141+3070G>C XP_011510609.1:n.141+3070G>C