Canonical Allele Identifier: CA440675966
Gene:

Linked Data

MyVariant Identifiers: chr4:g.106463797T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542640T>A , CM000666.2:g.105542640T>A GRCh38
NC_000004.11:g.106463797T>A , CM000666.1:g.106463797T>A GRCh37
NC_000004.10:g.106683246T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.365A>T
XR_939039.1:n.525A>T
XR_939040.1:n.296-1164A>T
XR_001741410.1:n.380A>T
XR_001741411.1:n.856A>T
XR_001741412.1:n.380A>T
XR_001741413.1:n.380A>T
XR_001741414.1:n.380A>T
XR_939038.2:n.380A>T
XR_939040.2:n.311-1164A>T