Canonical Allele Identifier: CA829129708
Gene:

Linked Data

dbSNP Id: rs1049047000

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.85982232G>T , CM000668.2:g.85982232G>T GRCh38
NC_000006.11:g.86691950G>T , CM000668.1:g.86691950G>T GRCh37
NC_000006.10:g.86748669G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_241869.3:n.615-11148G>T
XR_942747.1:n.41-1137G>T
XR_942748.1:n.27-1137G>T
XR_001744239.1:n.1570-11148G>T
XR_001744243.1:n.1433-11148G>T
XR_002956361.1:n.1992-11148G>T