Canonical Allele Identifier: CA348605621
Gene: LCT HGNC NCBI

Linked Data

dbSNP Id: rs2077788117

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135817366G>C , CM000664.2:g.135817366G>C GRCh38
NC_000002.11:g.136574936G>C , CM000664.1:g.136574936G>C GRCh37
NC_000002.10:g.136291406G>C NCBI36
NG_008104.2:g.42804C>G , LRG_338:g.42804C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.1682C>G MANE Select ENSP00000264162.2:p.Ser561Cys
ENST00000264162.6:c.1682C>G ENSP00000264162.2:p.Ser561Cys
NM_002299.2:c.1682C>G , LRG_338t1:c.1682C>G NP_002290.2:p.Ser561Cys
NM_002299.3:c.1682C>G NP_002290.2:p.Ser561Cys
XM_017004088.2:c.1682C>G XP_016859577.1:p.Ser561Cys
NM_002299.4:c.1682C>G MANE Select NP_002290.2:p.Ser561Cys