Canonical Allele Identifier: CA168427884
Gene:

Linked Data

dbSNP Id: rs952154168
gnomAD v2: 7-144841451-T-A
gnomAD v3: 7-145144358-T-A
gnomAD v4: 7-145144358-T-A
MyVariant Identifiers: chr7:g.144841451T>A (hg19) chr7:g.145144358T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.145144358T>A , CM000669.2:g.145144358T>A GRCh38
NC_000007.13:g.144841451T>A , CM000669.1:g.144841451T>A GRCh37
NC_000007.12:g.144472384T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928090.1:n.1968-12577T>A
XR_928090.2:n.4143-12577T>A
Search 100 bp 5'
Search 100 bp 3'