Canonical Allele Identifier: CA440675820
Gene:

Linked Data

MyVariant Identifiers: chr4:g.106463746T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542589T>C , CM000666.2:g.105542589T>C GRCh38
NC_000004.11:g.106463746T>C , CM000666.1:g.106463746T>C GRCh37
NC_000004.10:g.106683195T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.416A>G
XR_939039.1:n.576A>G
XR_939040.1:n.296-1113A>G
XR_001741410.1:n.431A>G
XR_001741411.1:n.907A>G
XR_001741412.1:n.431A>G
XR_001741413.1:n.431A>G
XR_001741414.1:n.431A>G
XR_939038.2:n.431A>G
XR_939040.2:n.311-1113A>G