Canonical Allele Identifier: CA1482798041
Gene:

Linked Data

dbSNP Id: rs538059088

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542964G>A , CM000666.2:g.105542964G>A GRCh38
NC_000004.11:g.106464121G>A , CM000666.1:g.106464121G>A GRCh37
NC_000004.10:g.106683570G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.296-255C>T
XR_939039.1:n.456-255C>T
XR_939040.1:n.296-1488C>T
XR_001741410.1:n.311-255C>T
XR_001741411.1:n.787-255C>T
XR_001741412.1:n.311-255C>T
XR_001741413.1:n.311-255C>T
XR_001741414.1:n.311-255C>T
XR_939038.2:n.311-255C>T
XR_939040.2:n.311-1488C>T