Canonical Allele Identifier: CA145433654
Gene: LIN28B HGNC NCBI

Linked Data

dbSNP Id: rs1016030669
gnomAD v2: 6-105404202-T-G
gnomAD v3: 6-104956327-T-G
gnomAD v4: 6-104956327-T-G
MyVariant Identifiers: chr6:g.105404202T>G (hg19) chr6:g.104956327T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.104956327T>G , CM000668.2:g.104956327T>G GRCh38
NC_000006.11:g.105404202T>G , CM000668.1:g.105404202T>G GRCh37
NC_000006.10:g.105510895T>G NCBI36
NG_032815.1:g.4280T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000635857.1:c.68-1772T>G ENSP00000489735.1:n.68-1772T>G
ENST00000637759.1:c.35-1772T>G ENSP00000490468.1:n.35-1772T>G
XM_006715477.2:c.68-1772T>G XP_006715540.2:n.68-1772T>G
XM_011535818.1:c.35-1772T>G XP_011534120.1:n.35-1772T>G
XM_011535818.3:c.35-1772T>G XP_011534120.1:n.35-1772T>G
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