Canonical Allele Identifier: CA788842533
Gene:

Linked Data

dbSNP Id: rs1378604507
MyVariant Identifiers: chr4:g.149570708T>G (hg19) chr4:g.148649556T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148649556T>G , CM000666.2:g.148649556T>G GRCh38
NC_000004.11:g.149570708T>G , CM000666.1:g.149570708T>G GRCh37
NC_000004.10:g.149790158T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939336.1:n.437-30688A>C
XR_001741441.1:n.1745+104972T>G
XR_939336.3:n.2921-30688A>C
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