Canonical Allele Identifier: CA440676031
Gene:

Linked Data

MyVariant Identifiers: chr4:g.106463820T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542663T>A , CM000666.2:g.105542663T>A GRCh38
NC_000004.11:g.106463820T>A , CM000666.1:g.106463820T>A GRCh37
NC_000004.10:g.106683269T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.342A>T
XR_939039.1:n.502A>T
XR_939040.1:n.296-1187A>T
XR_001741410.1:n.357A>T
XR_001741411.1:n.833A>T
XR_001741412.1:n.357A>T
XR_001741413.1:n.357A>T
XR_001741414.1:n.357A>T
XR_939038.2:n.357A>T
XR_939040.2:n.311-1187A>T