Canonical Allele Identifier: CA440675885
Gene:

Linked Data

MyVariant Identifiers: chr4:g.106463769T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542612T>A , CM000666.2:g.105542612T>A GRCh38
NC_000004.11:g.106463769T>A , CM000666.1:g.106463769T>A GRCh37
NC_000004.10:g.106683218T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.393A>T
XR_939039.1:n.553A>T
XR_939040.1:n.296-1136A>T
XR_001741410.1:n.408A>T
XR_001741411.1:n.884A>T
XR_001741412.1:n.408A>T
XR_001741413.1:n.408A>T
XR_001741414.1:n.408A>T
XR_939038.2:n.408A>T
XR_939040.2:n.311-1136A>T