Canonical Allele Identifier: CA683949573
Gene:

Linked Data

dbSNP Id: rs2194980

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.115064913A>T , CM000674.2:g.115064913A>T GRCh38
NC_000012.11:g.115502718A>T , CM000674.1:g.115502718A>T GRCh37
NC_000012.10:g.113987101A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945384.1:n.744-30192A>T
XR_945385.1:n.432+2056A>T
XR_001749329.1:n.537+2056A>T
XR_001749330.1:n.426-30192A>T
XR_001749333.1:n.1505+2056A>T
XR_001749334.1:n.426-12311A>T