Canonical Allele Identifier: CA396376123
Gene: LCAT HGNC NCBI

Linked Data

COSMIC: COSM117535
MyVariant Identifiers: chr16:g.67974238T>C (hg19) chr16:g.67940335T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940335T>C , CM000678.2:g.67940335T>C GRCh38
NC_000016.9:g.67974238T>C , CM000678.1:g.67974238T>C GRCh37
NC_000016.8:g.66531739T>C NCBI36
NG_009778.1:g.8778A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.892A>G MANE Select ENSP00000264005.5:p.Thr298Ala
ENST00000264005.9:c.892A>G ENSP00000264005.5:p.Thr298Ala
ENST00000570369.5:c.156-261A>G
ENST00000570980.1:c.676A>G ENSP00000464651.1:p.Thr226Ala
ENST00000573538.5:c.630A>G ENSP00000463220.1:n.630A>G
NM_000229.1:c.892A>G NP_000220.1:p.Thr298Ala
NM_000229.2:c.892A>G MANE Select NP_000220.1:p.Thr298Ala
Search 100 bp 5'
Search 100 bp 3'