Canonical Allele Identifier: CA13017001
Gene:

Linked Data

dbSNP Id: rs2422493
gnomAD v2: 9-107690995-G-A
gnomAD v3: 9-104928714-G-A
gnomAD v4: 9-104928714-G-A
MyVariant Identifiers: chr9:g.107690995G>A (hg19) chr9:g.104928714G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.104928714G>A , CM000671.2:g.104928714G>A GRCh38
NC_000009.11:g.107690995G>A , CM000671.1:g.107690995G>A GRCh37
NC_000009.10:g.106730816G>A NCBI36
NG_007981.1:g.4442C>T

Transcript Alleles

HGVS Amino-acid change
XR_930204.1:n.735-794G>A
XR_930204.2:n.116-794G>A
Search 100 bp 5'
Search 100 bp 3'