Canonical Allele Identifier: CA440676065
Gene:

Linked Data

MyVariant Identifiers: chr4:g.106463832A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542675A>T , CM000666.2:g.105542675A>T GRCh38
NC_000004.11:g.106463832A>T , CM000666.1:g.106463832A>T GRCh37
NC_000004.10:g.106683281A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.330T>A
XR_939039.1:n.490T>A
XR_939040.1:n.296-1199T>A
XR_001741410.1:n.345T>A
XR_001741411.1:n.821T>A
XR_001741412.1:n.345T>A
XR_001741413.1:n.345T>A
XR_001741414.1:n.345T>A
XR_939038.2:n.345T>A
XR_939040.2:n.311-1199T>A