Canonical Allele Identifier: CA197410905
Gene:

Linked Data

dbSNP Id: rs1013128162
gnomAD v3: 9-104928272-T-C
gnomAD v4: 9-104928272-T-C
MyVariant Identifiers: chr9:g.107690553T>C (hg19) chr9:g.104928272T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.104928272T>C , CM000671.2:g.104928272T>C GRCh38
NC_000009.11:g.107690553T>C , CM000671.1:g.107690553T>C GRCh37
NC_000009.10:g.106730374T>C NCBI36
NG_007981.1:g.4884A>G

Transcript Alleles

HGVS Amino-acid change
XR_930204.1:n.734+362T>C
XR_930204.2:n.115+362T>C
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