Canonical Allele Identifier: CA440676034
Gene:

Linked Data

MyVariant Identifiers: chr4:g.106463821G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542664G>A , CM000666.2:g.105542664G>A GRCh38
NC_000004.11:g.106463821G>A , CM000666.1:g.106463821G>A GRCh37
NC_000004.10:g.106683270G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.341C>T
XR_939039.1:n.501C>T
XR_939040.1:n.296-1188C>T
XR_001741410.1:n.356C>T
XR_001741411.1:n.832C>T
XR_001741412.1:n.356C>T
XR_001741413.1:n.356C>T
XR_001741414.1:n.356C>T
XR_939038.2:n.356C>T
XR_939040.2:n.311-1188C>T