Canonical Allele Identifier: CA440675801

Gene:

Linked Data

• dbSNP Id: rs2110367744
• MyVariant Identifiers: chr4:g.106463740G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.105542583G>A , CM000666.2:g.105542583G>A	GRCh38
NC_000004.11:g.106463740G>A , CM000666.1:g.106463740G>A	GRCh37
NC_000004.10:g.106683189G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_939038.1:n.422C>T
XR_939039.1:n.582C>T
XR_939040.1:n.296-1107C>T
XR_001741410.1:n.437C>T
XR_001741411.1:n.913C>T
XR_001741412.1:n.437C>T
XR_001741413.1:n.437C>T
XR_001741414.1:n.437C>T
XR_939038.2:n.437C>T
XR_939040.2:n.311-1107C>T