Canonical Allele Identifier: CA440675933

Gene:

Linked Data

• gnomAD v4: 4-105542628-C-T
• MyVariant Identifiers: chr4:g.106463785C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.105542628C>T , CM000666.2:g.105542628C>T	GRCh38
NC_000004.11:g.106463785C>T , CM000666.1:g.106463785C>T	GRCh37
NC_000004.10:g.106683234C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_939038.1:n.377G>A
XR_939039.1:n.537G>A
XR_939040.1:n.296-1152G>A
XR_001741410.1:n.392G>A
XR_001741411.1:n.868G>A
XR_001741412.1:n.392G>A
XR_001741413.1:n.392G>A
XR_001741414.1:n.392G>A
XR_939038.2:n.392G>A
XR_939040.2:n.311-1152G>A