Canonical Allele Identifier: CA429204489
Gene: LCT HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.136574944G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135817374G>C , CM000664.2:g.135817374G>C GRCh38
NC_000002.11:g.136574944G>C , CM000664.1:g.136574944G>C GRCh37
NC_000002.10:g.136291414G>C NCBI36
NG_008104.2:g.42796C>G , LRG_338:g.42796C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.1674C>G MANE Select ENSP00000264162.2:p.Pro558=
ENST00000264162.6:c.1674C>G ENSP00000264162.2:p.Pro558=
NM_002299.2:c.1674C>G , LRG_338t1:c.1674C>G NP_002290.2:p.Pro558=
NM_002299.3:c.1674C>G NP_002290.2:p.Pro558=
XM_017004088.2:c.1674C>G XP_016859577.1:p.Pro558=
NM_002299.4:c.1674C>G MANE Select NP_002290.2:p.Pro558=
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