Canonical Allele Identifier: CA1841175619
Gene:

Linked Data

dbSNP Id: rs1819677766
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551490C>T , CM000671.2:g.25551490C>T GRCh38
NC_000009.11:g.25551488C>T , CM000671.1:g.25551488C>T GRCh37
NC_000009.10:g.25541488C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-918G>A
XR_929525.2:n.674-918G>A
Search 100 bp 5'
Search 100 bp 3'