Canonical Allele Identifier: CA723098044
Gene: LCAT HGNC NCBI

Linked Data

dbSNP Id: rs1293658739
gnomAD v3: 16-67940687-T-C
gnomAD v4: 16-67940687-T-C
MyVariant Identifiers: chr16:g.67974590T>C (hg19) chr16:g.67940687T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940687T>C , CM000678.2:g.67940687T>C GRCh38
NC_000016.9:g.67974590T>C , CM000678.1:g.67974590T>C GRCh37
NC_000016.8:g.66532091T>C NCBI36
NG_009778.1:g.8426A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.749-209A>G MANE Select ENSP00000264005.5:n.749-209A>G
ENST00000264005.9:c.749-209A>G ENSP00000264005.5:n.749-209A>G
ENST00000570369.5:c.156-613A>G
ENST00000570980.1:c.533-209A>G ENSP00000464651.1:n.533-209A>G
ENST00000573538.5:c.486+50A>G ENSP00000463220.1:n.486+50A>G
NM_000229.1:c.749-209A>G NP_000220.1:n.749-209A>G
NM_000229.2:c.749-209A>G MANE Select NP_000220.1:n.749-209A>G
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