Canonical Allele Identifier: CA2210126531
Gene:

Linked Data

dbSNP Id: rs2046233032
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16143936G>A , CM000678.2:g.16143936G>A GRCh38
NC_000016.9:g.16237793G>A , CM000678.1:g.16237793G>A GRCh37
NC_000016.8:g.16145294G>A NCBI36
NG_028268.1:g.199360G>A
NG_028268.2:g.199360G>A

Transcript Alleles

HGVS Amino-acid change
XR_933134.1:n.184G>A
Search 100 bp 5'
Search 100 bp 3'