Canonical Allele Identifier: CA440675841

Gene:

Linked Data

• dbSNP Id: rs1724781385
• MyVariant Identifiers: chr4:g.106463753A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.105542596A>G , CM000666.2:g.105542596A>G	GRCh38
NC_000004.11:g.106463753A>G , CM000666.1:g.106463753A>G	GRCh37
NC_000004.10:g.106683202A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_939038.1:n.409T>C
XR_939039.1:n.569T>C
XR_939040.1:n.296-1120T>C
XR_001741410.1:n.424T>C
XR_001741411.1:n.900T>C
XR_001741412.1:n.424T>C
XR_001741413.1:n.424T>C
XR_001741414.1:n.424T>C
XR_939038.2:n.424T>C
XR_939040.2:n.311-1120T>C