Canonical Allele Identifier: CA721927966
Gene:

Linked Data

dbSNP Id: rs1297104208

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55655460A>C , CM000678.2:g.55655460A>C GRCh38
NC_000016.9:g.55689372A>C , CM000678.1:g.55689372A>C GRCh37
NC_000016.8:g.54246873A>C NCBI36
NG_016969.1:g.4831A>C

Transcript Alleles

HGVS Amino-acid Change
XR_933603.1:n.54+139T>G