Canonical Allele Identifier: CA429086214
Gene: LCT HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.136555673C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135798103C>T , CM000664.2:g.135798103C>T GRCh38
NC_000002.11:g.136555673C>T , CM000664.1:g.136555673C>T GRCh37
NC_000002.10:g.136272143C>T NCBI36
NG_008104.2:g.62067G>A , LRG_338:g.62067G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.4902G>A MANE Select ENSP00000264162.2:p.Lys1634=
ENST00000264162.6:c.4902G>A ENSP00000264162.2:p.Lys1634=
ENST00000452974.1:c.2995G>A ENSP00000391231.1:p.Glu999Lys
NM_002299.2:c.4902G>A , LRG_338t1:c.4902G>A NP_002290.2:p.Lys1634=
NM_002299.3:c.4902G>A NP_002290.2:p.Lys1634=
XM_017004088.2:c.4902G>A XP_016859577.1:p.Lys1634=
NM_002299.4:c.4902G>A MANE Select NP_002290.2:p.Lys1634=