Canonical Allele Identifier: CA1066321140
Gene:

Linked Data

dbSNP Id: rs1724780663

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542559G>T , CM000666.2:g.105542559G>T GRCh38
NC_000004.11:g.106463716G>T , CM000666.1:g.106463716G>T GRCh37
NC_000004.10:g.106683165G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939038.1:n.446C>A
XR_939039.1:n.606C>A
XR_939040.1:n.296-1083C>A
XR_001741410.1:n.461C>A
XR_001741411.1:n.937C>A
XR_001741412.1:n.449+12C>A
XR_001741413.1:n.461C>A
XR_001741414.1:n.449+12C>A
XR_939038.2:n.461C>A
XR_939040.2:n.311-1083C>A