Canonical Allele Identifier: CA396375701
Gene: LCAT HGNC NCBI

Linked Data

dbSNP Id: rs1278725445
gnomAD v3: 16-67940133-T-C
gnomAD v4: 16-67940133-T-C
MyVariant Identifiers: chr16:g.67974036T>C (hg19) chr16:g.67940133T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940133T>C , CM000678.2:g.67940133T>C GRCh38
NC_000016.9:g.67974036T>C , CM000678.1:g.67974036T>C GRCh37
NC_000016.8:g.66531537T>C NCBI36
NG_009778.1:g.8980A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.1094A>G MANE Select ENSP00000264005.5:p.Tyr365Cys
ENST00000264005.9:c.1094A>G ENSP00000264005.5:p.Tyr365Cys
ENST00000570369.5:c.156-59A>G
ENST00000573538.5:c.832A>G ENSP00000463220.1:n.832A>G
NM_000229.1:c.1094A>G NP_000220.1:p.Tyr365Cys
NM_000229.2:c.1094A>G MANE Select NP_000220.1:p.Tyr365Cys
Search 100 bp 5'
Search 100 bp 3'