Canonical Allele Identifier: CA99746706
Gene:

Linked Data

dbSNP Id: rs184477487
gnomAD v3: 4-74304457-T-A
gnomAD v4: 4-74304457-T-A
MyVariant Identifiers: chr4:g.75170174T>A (hg19) chr4:g.74304457T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.74304457T>A , CM000666.2:g.74304457T>A GRCh38
NC_000004.11:g.75170174T>A , CM000666.1:g.75170174T>A GRCh37
NC_000004.10:g.75389038T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938877.1:n.120-25679A>T
XR_938877.2:n.126-25679A>T
Search 100 bp 5'
Search 100 bp 3'