Canonical Allele Identifier: CA798375083
Gene:

Linked Data

dbSNP Id: rs1297736169
MyVariant Identifiers: chr4:g.74554219G>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.74554219G>C , CM000666.2:g.74554219G>C GRCh38
NC_000004.11:g.75419936G>C , CM000666.1:g.75419936G>C GRCh37
NC_000004.10:g.75638800G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001741513.1:n.167-1387C>G