Canonical Allele Identifier: CA15434592

Gene: LIN28B

Linked Data

• dbSNP Id: rs314276
• gnomAD v2: 6-105407999-A-C
• gnomAD v3: 6-104960124-A-C
• gnomAD v4: 6-104960124-A-C
• MyVariant Identifiers: chr6:g.105407999A>C (hg19) ; chr6:g.104960124A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.104960124A>C , CM000668.2:g.104960124A>C	GRCh38
NC_000006.11:g.105407999A>C , CM000668.1:g.105407999A>C	GRCh37
NC_000006.10:g.105514692A>C	NCBI36
NG_032815.1:g.8077A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345080.5:c.198+1838A>C MANE Select	ENSP00000344401.4:n.198+1838A>C
ENST00000635857.1:c.255+1838A>C	ENSP00000489735.1:n.255+1838A>C
ENST00000637759.1:c.222+1838A>C	ENSP00000490468.1:n.222+1838A>C
ENST00000345080.4:c.198+1838A>C	ENSP00000344401.4:n.198+1838A>C
NM_001004317.3:c.198+1838A>C	NP_001004317.1:n.198+1838A>C
XM_006715477.2:c.255+1838A>C	XP_006715540.2:n.255+1838A>C
XM_011535818.1:c.222+1838A>C	XP_011534120.1:n.222+1838A>C
XM_011535818.3:c.222+1838A>C	XP_011534120.1:n.222+1838A>C
NM_001004317.4:c.198+1838A>C MANE Select	NP_001004317.1:n.198+1838A>C