Canonical Allele Identifier: CA39003139
Gene:

Linked Data

dbSNP Id: rs890956733
gnomAD v2: 1-225074807-T-G
gnomAD v3: 1-224887105-T-G
gnomAD v4: 1-224887105-T-G
MyVariant Identifiers: chr1:g.225074807T>G (hg19) chr1:g.224887105T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.224887105T>G , CM000663.2:g.224887105T>G GRCh38
NC_000001.10:g.225074807T>G , CM000663.1:g.225074807T>G GRCh37
NC_000001.9:g.223141430T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949207.1:n.66-2324A>C
XR_949207.2:n.63-2324A>C
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