Canonical Allele Identifier: CA440675838
Gene:

Linked Data

MyVariant Identifiers: chr4:g.106463752C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542595C>T , CM000666.2:g.105542595C>T GRCh38
NC_000004.11:g.106463752C>T , CM000666.1:g.106463752C>T GRCh37
NC_000004.10:g.106683201C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.410G>A
XR_939039.1:n.570G>A
XR_939040.1:n.296-1119G>A
XR_001741410.1:n.425G>A
XR_001741411.1:n.901G>A
XR_001741412.1:n.425G>A
XR_001741413.1:n.425G>A
XR_001741414.1:n.425G>A
XR_939038.2:n.425G>A
XR_939040.2:n.311-1119G>A
Search 100 bp 5'
Search 100 bp 3'