Canonical Allele Identifier: CA496092310
Gene: LCAT HGNC NCBI

Linked Data

dbSNP Id: rs1354925358
gnomAD v2: 16-67973873-C-G
gnomAD v4: 16-67939970-C-G
MyVariant Identifiers: chr16:g.67973873C>G (hg19) chr16:g.67939970C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67939970C>G , CM000678.2:g.67939970C>G GRCh38
NC_000016.9:g.67973873C>G , CM000678.1:g.67973873C>G GRCh37
NC_000016.8:g.66531374C>G NCBI36
NG_009778.1:g.9143G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.1257G>C MANE Select ENSP00000264005.5:p.Leu419=
ENST00000264005.9:c.1257G>C ENSP00000264005.5:p.Leu419=
ENST00000570369.5:c.260G>C
ENST00000573538.5:c.995G>C ENSP00000463220.1:n.995G>C
NM_000229.1:c.1257G>C NP_000220.1:p.Leu419=
NM_000229.2:c.1257G>C MANE Select NP_000220.1:p.Leu419=
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Search 100 bp 3'