Canonical Allele Identifier: CA586881662
Gene:

Linked Data

dbSNP Id: rs1179813828
gnomAD v2: 9-21756076-C-T
gnomAD v3: 9-21756077-C-T
gnomAD v4: 9-21756077-C-T
MyVariant Identifiers: chr9:g.21756076C>T (hg19) chr9:g.21756077C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21756077C>T , CM000671.2:g.21756077C>T GRCh38
NC_000009.11:g.21756076C>T , CM000671.1:g.21756076C>T GRCh37
NC_000009.10:g.21746076C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746563.2:n.163+11748G>A
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