Canonical Allele Identifier: CA1581765790
Gene:

Linked Data

dbSNP Id: rs1476100887

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.129386841T>C , CM000667.2:g.129386841T>C GRCh38
NC_000005.9:g.128722534T>C , CM000667.1:g.128722534T>C GRCh37
NC_000005.8:g.128750433T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427770.2:n.163-1607T>C
XR_948774.1:n.235-5810T>C
XR_001742463.1:n.4089-1607T>C
XR_001742464.1:n.2019-5810T>C
XR_001742465.1:n.401-1607T>C
XR_427770.3:n.337-1607T>C