Canonical Allele Identifier: CA10739170
Gene:

Linked Data

dbSNP Id: rs3126085

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152328341G>A , CM000663.2:g.152328341G>A GRCh38
NC_000001.10:g.152300817G>A , CM000663.1:g.152300817G>A GRCh37
NC_000001.9:g.150567441G>A NCBI36
NG_016190.1:g.1863C>T , LRG_1028:g.1863C>T

Transcript Alleles

HGVS Amino-acid change
NR_103778.1:n.915-4242G>A