Canonical Allele Identifier: CA396375752
Gene: LCAT HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.67974061A>G (hg19) chr16:g.67940158A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940158A>G , CM000678.2:g.67940158A>G GRCh38
NC_000016.9:g.67974061A>G , CM000678.1:g.67974061A>G GRCh37
NC_000016.8:g.66531562A>G NCBI36
NG_009778.1:g.8955T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.1069T>C MANE Select ENSP00000264005.5:p.Tyr357His
ENST00000264005.9:c.1069T>C ENSP00000264005.5:p.Tyr357His
ENST00000570369.5:c.156-84T>C
ENST00000573538.5:c.807T>C ENSP00000463220.1:n.807T>C
NM_000229.1:c.1069T>C NP_000220.1:p.Tyr357His
NM_000229.2:c.1069T>C MANE Select NP_000220.1:p.Tyr357His
Search 100 bp 5'
Search 100 bp 3'