Canonical Allele Identifier: CA1163454599
Gene:

Linked Data

dbSNP Id: rs1642173951
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.38168074G>A , CM000663.2:g.38168074G>A GRCh38
NC_000001.10:g.38633746G>A , CM000663.1:g.38633746G>A GRCh37
NC_000001.9:g.38406333G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_947202.1:n.175+6251G>A
XR_947203.1:n.62-24931G>A
XR_947204.1:n.175+6251G>A
XR_947205.1:n.175+6251G>A
XR_001737984.1:n.175+6251G>A
XR_001737985.1:n.62-24931G>A
XR_001737986.1:n.175+6251G>A
XR_001737987.1:n.175+6251G>A
XR_002958294.1:n.175+6251G>A
XR_947205.2:n.175+6251G>A
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