Canonical Allele Identifier: CA98367564
Gene:

Linked Data

dbSNP Id: rs1017550060
MyVariant Identifiers: chr4:g.62558184G>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558184G>T , CM000666.2:g.62558184G>T GRCh38
NC_000004.11:g.63423902G>T , CM000666.1:g.63423902G>T GRCh37
NC_000004.10:g.63106497G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5660G>T