Canonical Allele Identifier: CA440675792
Gene:

Linked Data

MyVariant Identifiers: chr4:g.106463737A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542580A>C , CM000666.2:g.105542580A>C GRCh38
NC_000004.11:g.106463737A>C , CM000666.1:g.106463737A>C GRCh37
NC_000004.10:g.106683186A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939038.1:n.425T>G
XR_939039.1:n.585T>G
XR_939040.1:n.296-1104T>G
XR_001741410.1:n.440T>G
XR_001741411.1:n.916T>G
XR_001741412.1:n.440T>G
XR_001741413.1:n.440T>G
XR_001741414.1:n.440T>G
XR_939038.2:n.440T>G
XR_939040.2:n.311-1104T>G