Canonical Allele Identifier: CA1678638497
Gene:

Linked Data

dbSNP Id: rs1780708050

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.163765657G>T , CM000668.2:g.163765657G>T GRCh38
NC_000006.11:g.164186689G>T , CM000668.1:g.164186689G>T GRCh37
NC_000006.10:g.164106679G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001744452.1:n.410+6228G>T
XR_001744454.1:n.369+6269G>T
XR_001744455.1:n.346+6292G>T