Canonical Allele Identifier: CA798374979
Gene:

Linked Data

dbSNP Id: rs1487990670
gnomAD v3: 4-74554017-A-C
gnomAD v4: 4-74554017-A-C
MyVariant Identifiers: chr4:g.74554017A>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.74554017A>C , CM000666.2:g.74554017A>C GRCh38
NC_000004.11:g.75419734A>C , CM000666.1:g.75419734A>C GRCh37
NC_000004.10:g.75638598A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001741513.1:n.167-1185T>G