Canonical Allele Identifier: CA732182696
Gene:

Linked Data

dbSNP Id: rs1173018582
MyVariant Identifiers: chr1:g.225074723G>A (hg19) chr1:g.224887021G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.224887021G>A , CM000663.2:g.224887021G>A GRCh38
NC_000001.10:g.225074723G>A , CM000663.1:g.225074723G>A GRCh37
NC_000001.9:g.223141346G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949207.1:n.66-2240C>T
XR_949207.2:n.63-2240C>T
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