Canonical Allele Identifier: CA158302402
Gene:

Linked Data

dbSNP Id: rs574593943
MyVariant Identifiers: chr7:g.46072478T>C (hg19) chr7:g.46032880T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.46032880T>C , CM000669.2:g.46032880T>C GRCh38
NC_000007.13:g.46072478T>C , CM000669.1:g.46072478T>C GRCh37
NC_000007.12:g.46039003T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745203.1:n.1270-3738T>C
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