Canonical Allele Identifier: CA297885452
Gene:

Linked Data

dbSNP Id: rs1420956

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.27587981T>C , CM000680.2:g.27587981T>C GRCh38
NC_000018.9:g.25167945T>C , CM000680.1:g.25167945T>C GRCh37
NC_000018.8:g.23421943T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001753533.1:n.247+4842A>G
XR_001753534.1:n.247+4842A>G
XR_001753535.1:n.196-5966A>G
XR_001753536.1:n.196-5966A>G