Canonical Allele Identifier: CA190667314
Gene:

Linked Data

dbSNP Id: rs868493454
MyVariant Identifiers: chr9:g.21755989C>T (hg19) chr9:g.21755990C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21755990C>T , CM000671.2:g.21755990C>T GRCh38
NC_000009.11:g.21755989C>T , CM000671.1:g.21755989C>T GRCh37
NC_000009.10:g.21745989C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746563.2:n.163+11835G>A
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