Canonical Allele Identifier: CA1216113102
Gene:

Linked Data

dbSNP Id: rs1257883578
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193121741A>T , CM000663.2:g.193121741A>T GRCh38
NC_000001.10:g.193090871A>T , CM000663.1:g.193090871A>T GRCh37
NC_000001.9:g.191357494A>T NCBI36
NG_012691.1:g.4784A>T , LRG_507:g.4784A>T

Transcript Alleles

HGVS Amino-acid Change
XR_001738350.1:n.1916T>A
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