Canonical Allele Identifier: CA788849987
Gene:

Linked Data

dbSNP Id: rs1247612870
MyVariant Identifiers: chr4:g.149669525A>C (hg19) chr4:g.148748373A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148748373A>C , CM000666.2:g.148748373A>C GRCh38
NC_000004.11:g.149669525A>C , CM000666.1:g.149669525A>C GRCh37
NC_000004.10:g.149888975A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001741441.1:n.1746-118384A>C
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