Canonical Allele Identifier: CA784842409

Gene:

Linked Data

• dbSNP Id: rs1425371011
• gnomAD v4: 4-105542834-G-T
• MyVariant Identifiers: chr4:g.106463991G>T (hg19) ; chr4:g.105542834G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.105542834G>T , CM000666.2:g.105542834G>T	GRCh38
NC_000004.11:g.106463991G>T , CM000666.1:g.106463991G>T	GRCh37
NC_000004.10:g.106683440G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_939038.1:n.296-125C>A
XR_939039.1:n.456-125C>A
XR_939040.1:n.296-1358C>A
XR_001741410.1:n.311-125C>A
XR_001741411.1:n.787-125C>A
XR_001741412.1:n.311-125C>A
XR_001741413.1:n.311-125C>A
XR_001741414.1:n.311-125C>A
XR_939038.2:n.311-125C>A
XR_939040.2:n.311-1358C>A