Canonical Allele Identifier: CA396376029
Gene: LCAT HGNC NCBI

Linked Data

gnomAD v4: 16-67940292-T-C
MyVariant Identifiers: chr16:g.67974195T>C (hg19) chr16:g.67940292T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940292T>C , CM000678.2:g.67940292T>C GRCh38
NC_000016.9:g.67974195T>C , CM000678.1:g.67974195T>C GRCh37
NC_000016.8:g.66531696T>C NCBI36
NG_009778.1:g.8821A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264005.10:c.935A>G MANE Select ENSP00000264005.5:p.Glu312Gly
ENST00000264005.9:c.935A>G ENSP00000264005.5:p.Glu312Gly
ENST00000570369.5:c.156-218A>G
ENST00000570980.1:c.719A>G ENSP00000464651.1:p.Glu240Gly
ENST00000573538.5:c.673A>G ENSP00000463220.1:n.673A>G
NM_000229.1:c.935A>G NP_000220.1:p.Glu312Gly
NM_000229.2:c.935A>G MANE Select NP_000220.1:p.Glu312Gly
Search 100 bp 5'
Search 100 bp 3'