Canonical Allele Identifier: CA396376396
Gene: LCAT HGNC NCBI

Linked Data

gnomAD v4: 16-67940456-G-C
MyVariant Identifiers: chr16:g.67974359G>C (hg19) chr16:g.67940456G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940456G>C , CM000678.2:g.67940456G>C GRCh38
NC_000016.9:g.67974359G>C , CM000678.1:g.67974359G>C GRCh37
NC_000016.8:g.66531860G>C NCBI36
NG_009778.1:g.8657C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.771C>G MANE Select ENSP00000264005.5:p.Ile257Met
ENST00000264005.9:c.771C>G ENSP00000264005.5:p.Ile257Met
ENST00000570369.5:c.156-382C>G
ENST00000570980.1:c.555C>G ENSP00000464651.1:p.Ile185Met
ENST00000573538.5:c.509C>G ENSP00000463220.1:n.509C>G
NM_000229.1:c.771C>G NP_000220.1:p.Ile257Met
NM_000229.2:c.771C>G MANE Select NP_000220.1:p.Ile257Met
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