Canonical Allele Identifier: CA396375744
Gene: LCAT HGNC NCBI

Linked Data

dbSNP Id: rs2058284553
MyVariant Identifiers: chr16:g.67974058T>C (hg19) chr16:g.67940155T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940155T>C , CM000678.2:g.67940155T>C GRCh38
NC_000016.9:g.67974058T>C , CM000678.1:g.67974058T>C GRCh37
NC_000016.8:g.66531559T>C NCBI36
NG_009778.1:g.8958A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.1072A>G MANE Select ENSP00000264005.5:p.Thr358Ala
ENST00000264005.9:c.1072A>G ENSP00000264005.5:p.Thr358Ala
ENST00000570369.5:c.156-81A>G
ENST00000573538.5:c.810A>G ENSP00000463220.1:n.810A>G
NM_000229.1:c.1072A>G NP_000220.1:p.Thr358Ala
NM_000229.2:c.1072A>G MANE Select NP_000220.1:p.Thr358Ala
Search 100 bp 5'
Search 100 bp 3'