Canonical Allele Identifier: CA396375458
Gene: LCAT HGNC NCBI

Linked Data

gnomAD v4: 16-67940016-A-G
MyVariant Identifiers: chr16:g.67973919A>G (hg19) chr16:g.67940016A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940016A>G , CM000678.2:g.67940016A>G GRCh38
NC_000016.9:g.67973919A>G , CM000678.1:g.67973919A>G GRCh37
NC_000016.8:g.66531420A>G NCBI36
NG_009778.1:g.9097T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.1211T>C MANE Select ENSP00000264005.5:p.Met404Thr
ENST00000264005.9:c.1211T>C ENSP00000264005.5:p.Met404Thr
ENST00000570369.5:c.214T>C
ENST00000573538.5:c.949T>C ENSP00000463220.1:n.949T>C
NM_000229.1:c.1211T>C NP_000220.1:p.Met404Thr
NM_000229.2:c.1211T>C MANE Select NP_000220.1:p.Met404Thr
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