Canonical Allele Identifier: CA440675934

Gene:

Linked Data

• gnomAD v4: 4-105542629-C-A
• MyVariant Identifiers: chr4:g.106463786C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.105542629C>A , CM000666.2:g.105542629C>A	GRCh38
NC_000004.11:g.106463786C>A , CM000666.1:g.106463786C>A	GRCh37
NC_000004.10:g.106683235C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_939038.1:n.376G>T
XR_939039.1:n.536G>T
XR_939040.1:n.296-1153G>T
XR_001741410.1:n.391G>T
XR_001741411.1:n.867G>T
XR_001741412.1:n.391G>T
XR_001741413.1:n.391G>T
XR_001741414.1:n.391G>T
XR_939038.2:n.391G>T
XR_939040.2:n.311-1153G>T