Canonical Allele Identifier: CA107748656
Gene:

Linked Data

dbSNP Id: rs9998537
MyVariant Identifiers: chr4:g.145480644T>G (hg19) chr4:g.144559492T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144559492T>G , CM000666.2:g.144559492T>G GRCh38
NC_000004.11:g.145480644T>G , CM000666.1:g.145480644T>G GRCh37
NC_000004.10:g.145700094T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649263.1:c.328-143514A>C ENSP00000497507.1:n.328-143514A>C
XR_939272.1:n.178+2492A>C
XR_939273.1:n.178+2492A>C
XR_939272.2:n.522+2492A>C
XR_939273.2:n.522+2492A>C
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