Canonical Allele Identifier: CA402379013

Gene: LOXHD1

Linked Data

• dbSNP Id: rs903294457
• gnomAD v2: 18-44159666-C-T
• gnomAD v4: 18-46579703-C-T
• MyVariant Identifiers: chr18:g.44159666C>T (hg19) ; chr18:g.46579703C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.46579703C>T , CM000680.2:g.46579703C>T	GRCh38
NC_000018.9:g.44159666C>T , CM000680.1:g.44159666C>T	GRCh37
NC_000018.8:g.42413664C>T	NCBI36
NG_016646.1:g.82331G>A
NG_016646.2:g.82331G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642948.1:c.1736G>A MANE Select	ENSP00000496347.1:p.Gly579Asp
ENST00000335730.6:n.1049G>A
ENST00000441551.6:c.1736G>A	ENSP00000387621.2:p.Gly579Asp
ENST00000536736.5:c.1736G>A	ENSP00000444586.1:p.Gly579Asp
NM_144612.6:c.1736G>A	NP_653213.6:p.Gly579Asp
XM_011525803.1:c.1736G>A	XP_011524105.1:p.Gly579Asp
XM_011525804.1:c.-30-1836G>A	XP_011524106.1:n.-30-1836G>A
XM_011525804.2:c.-30-1836G>A	XP_011524106.1:n.-30-1836G>A
XM_017025548.1:c.1736G>A	XP_016881037.1:p.Gly579Asp
XM_024451084.1:c.218G>A	XP_024306852.1:p.Gly73Asp
NM_001384474.1:c.1736G>A MANE Select	NP_001371403.1:p.Gly579Asp
NM_144612.7:c.1736G>A	NP_653213.6:p.Gly579Asp