Canonical Allele Identifier: CA440675779
Gene:

Linked Data

MyVariant Identifiers: chr4:g.106463732T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542575T>G , CM000666.2:g.105542575T>G GRCh38
NC_000004.11:g.106463732T>G , CM000666.1:g.106463732T>G GRCh37
NC_000004.10:g.106683181T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939038.1:n.430A>C
XR_939039.1:n.590A>C
XR_939040.1:n.296-1099A>C
XR_001741410.1:n.445A>C
XR_001741411.1:n.921A>C
XR_001741412.1:n.445A>C
XR_001741413.1:n.445A>C
XR_001741414.1:n.445A>C
XR_939038.2:n.445A>C
XR_939040.2:n.311-1099A>C