Canonical Allele Identifier: CA496092734
Gene: LCAT HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.67973966T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940063T>A , CM000678.2:g.67940063T>A GRCh38
NC_000016.9:g.67973966T>A , CM000678.1:g.67973966T>A GRCh37
NC_000016.8:g.66531467T>A NCBI36
NG_009778.1:g.9050A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.1164A>T MANE Select ENSP00000264005.5:p.Pro388=
ENST00000264005.9:c.1164A>T ENSP00000264005.5:p.Pro388=
ENST00000570369.5:c.167A>T
ENST00000573538.5:c.902A>T ENSP00000463220.1:n.902A>T
NM_000229.1:c.1164A>T NP_000220.1:p.Pro388=
NM_000229.2:c.1164A>T MANE Select NP_000220.1:p.Pro388=
Search 100 bp 5'
Search 100 bp 3'