Canonical Allele Identifier: CA15081606
Gene: LIN28A HGNC NCBI

Linked Data

dbSNP Id: rs6598964
gnomAD v2: 1-26746327-A-G
gnomAD v3: 1-26419836-A-G
gnomAD v4: 1-26419836-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26419836A>G , CM000663.2:g.26419836A>G GRCh38
NC_000001.10:g.26746327A>G , CM000663.1:g.26746327A>G GRCh37
NC_000001.9:g.26618914A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000326279.11:c.229-5467A>G MANE Select ENSP00000363314.3:n.229-5467A>G
ENST00000254231.4:c.229-5467A>G ENSP00000254231.4:n.229-5467A>G
ENST00000326279.10:c.229-5467A>G ENSP00000363314.3:n.229-5467A>G
NM_024674.4:c.229-5467A>G NP_078950.1:n.229-5467A>G
NM_024674.5:c.229-5467A>G NP_078950.1:n.229-5467A>G
XM_011542148.1:c.229-5467A>G XP_011540450.1:n.229-5467A>G
XM_011542148.2:c.229-5467A>G XP_011540450.1:n.229-5467A>G
NM_024674.6:c.229-5467A>G MANE Select NP_078950.1:n.229-5467A>G