Canonical Allele Identifier: CA99671581

Gene: AFP

Linked Data

• dbSNP Id: rs763054422
• MyVariant Identifiers: chr4:g.74308072G>T (hg19) ; chr4:g.73442355G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73442355G>T , CM000666.2:g.73442355G>T	GRCh38
NC_000004.11:g.74308072G>T , CM000666.1:g.74308072G>T	GRCh37
NC_000004.10:g.74526936G>T	NCBI36
NG_023028.1:g.11140G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395792.7:c.542G>T MANE Select	ENSP00000379138.2:p.Trp181Leu
ENST00000226359.2:c.542G>T	ENSP00000226359.2:p.Trp181Leu
ENST00000395792.6:c.542G>T	ENSP00000379138.2:p.Trp181Leu
NM_001134.2:c.542G>T	NP_001125.1:p.Trp181Leu
XM_011531704.1:c.539G>T	XP_011530006.1:p.Trp180Leu
NM_001354717.1:c.68G>T	NP_001341646.1:p.Trp23Leu
NM_001134.3:c.542G>T MANE Select	NP_001125.1:p.Trp181Leu
NM_001354717.2:c.68G>T	NP_001341646.2:p.Trp23Leu