Canonical Allele Identifier: CA102637954
Gene:

Linked Data

dbSNP Id: rs758399828
MyVariant Identifiers: chr4:g.100395344A>C (hg19) chr4:g.99474187A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99474187A>C , CM000666.2:g.99474187A>C GRCh38
NC_000004.11:g.100395344A>C , CM000666.1:g.100395344A>C GRCh37
NC_000004.10:g.100614367A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000506494.1:n.243-2325T>G
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