Canonical Allele Identifier: CA396375338
Gene: LCAT HGNC NCBI

Linked Data

dbSNP Id: rs2151319807
MyVariant Identifiers: chr16:g.67973864G>C (hg19) chr16:g.67939961G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67939961G>C , CM000678.2:g.67939961G>C GRCh38
NC_000016.9:g.67973864G>C , CM000678.1:g.67973864G>C GRCh37
NC_000016.8:g.66531365G>C NCBI36
NG_009778.1:g.9152C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.1266C>G MANE Select ENSP00000264005.5:p.Tyr422Ter
ENST00000264005.9:c.1266C>G ENSP00000264005.5:p.Tyr422Ter
ENST00000570369.5:c.269C>G
ENST00000573538.5:c.1004C>G ENSP00000463220.1:n.1004C>G
NM_000229.1:c.1266C>G NP_000220.1:p.Tyr422Ter
NM_000229.2:c.1266C>G MANE Select NP_000220.1:p.Tyr422Ter
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