Canonical Allele Identifier: CA26899207
Gene:

Linked Data

dbSNP Id: rs978572414
MyVariant Identifiers: chr1:g.95029611G>A (hg19) chr1:g.94564055G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94564055G>A , CM000663.2:g.94564055G>A GRCh38
NC_000001.10:g.95029611G>A , CM000663.1:g.95029611G>A GRCh37
NC_000001.9:g.94802199G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001738161.1:n.461+442G>A
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