Canonical Allele Identifier: CA2712751406
Gene:

Linked Data

dbSNP Id: rs2127980501

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98102443G>T , CM000668.2:g.98102443G>T GRCh38
NC_000006.11:g.98550319G>T , CM000668.1:g.98550319G>T GRCh37
NC_000006.10:g.98657040G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245563.2:n.456+3173G>T
XR_942809.1:n.456+3173G>T