Canonical Allele Identifier: CA798374958
Gene:

Linked Data

dbSNP Id: rs1386462199
gnomAD v3: 4-74553979-C-A
gnomAD v4: 4-74553979-C-A
MyVariant Identifiers: chr4:g.74553979C>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.74553979C>A , CM000666.2:g.74553979C>A GRCh38
NC_000004.11:g.75419696C>A , CM000666.1:g.75419696C>A GRCh37
NC_000004.10:g.75638560C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001741513.1:n.167-1147G>T