Canonical Allele Identifier: CA2210126512
Gene:

Linked Data

dbSNP Id: rs2046232160

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16143906T>C , CM000678.2:g.16143906T>C GRCh38
NC_000016.9:g.16237763T>C , CM000678.1:g.16237763T>C GRCh37
NC_000016.8:g.16145264T>C NCBI36
NG_028268.1:g.199330T>C
NG_028268.2:g.199330T>C

Transcript Alleles

HGVS Amino-acid change
XR_933134.1:n.154T>C