Canonical Allele Identifier: CA1339330530
Gene:

Linked Data

dbSNP Id: rs1575706912

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868459G>T , CM000664.2:g.240868459G>T GRCh38
NC_000002.11:g.241807876G>T , CM000664.1:g.241807876G>T GRCh37
NC_000002.10:g.241456549G>T NCBI36
NG_008005.1:g.4715G>T

Transcript Alleles

HGVS Amino-acid Change
XR_924060.1:n.405+1774C>A