Canonical Allele Identifier: CA119097043
Gene:

Linked Data

dbSNP Id: rs375765266
MyVariant Identifiers: chr5:g.56195796G>A (hg19) chr5:g.56899969G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56899969G>A , CM000667.2:g.56899969G>A GRCh38
NC_000005.9:g.56195796G>A , CM000667.1:g.56195796G>A GRCh37
NC_000005.8:g.56231553G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948346.1:n.83-1673C>T
XR_948347.1:n.76+28C>T
XR_948347.3:n.406+28C>T
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