Canonical Allele Identifier: CA423030937
Gene: LAMB3 HGNC NCBI
MIR4260 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.209796791T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209623446T>G , CM000663.2:g.209623446T>G GRCh38
NC_000001.10:g.209796791T>G , CM000663.1:g.209796791T>G GRCh37
NC_000001.9:g.207863414T>G NCBI36
NG_007116.1:g.34030A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000356082.9:c.2358+59A>C (LAMB3) MANE Select ENSP00000348384.3:n.2358+59A>C
ENST00000356082.8:c.2358+59A>C (LAMB3) ENSP00000348384.3:n.2358+59A>C
ENST00000367030.7:c.2358+59A>C (LAMB3) ENSP00000355997.3:n.2358+59A>C
ENST00000391911.5:c.2358+59A>C (LAMB3) ENSP00000375778.1:n.2358+59A>C
NM_000228.2:c.2358+59A>C (LAMB3) NP_000219.2:n.2358+59A>C
NM_001017402.1:c.2358+59A>C (LAMB3) NP_001017402.1:n.2358+59A>C
NM_001127641.1:c.2358+59A>C (LAMB3) NP_001121113.1:n.2358+59A>C
NR_036213.1:n.65A>C (MIR4260)
XM_005273124.3:c.2358+59A>C (LAMB3) XP_005273181.1:n.2358+59A>C
XM_005273124.4:c.2358+59A>C (LAMB3) XP_005273181.1:n.2358+59A>C
XM_017001272.2:c.2166+59A>C (LAMB3) XP_016856761.1:n.2166+59A>C
NM_000228.3:c.2358+59A>C (LAMB3) MANE Select NP_000219.2:n.2358+59A>C
NM_001017402.2:c.2358+59A>C (LAMB3) NP_001017402.1:n.2358+59A>C
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