Canonical Allele Identifier: CA15255218
Gene: LSM3 HGNC NCBI
MyVariant.info:
GRCh38 chr3:g.14178939C>T
GRCh37 chr3:g.14220439C>T
gnomAD v2:
3:14220439 C / T
gnomAD v3:
3:14178939 C / T
gnomAD v4:
chr3-14178939-C-T
Joint Max Group AF 0.21155414 (EAS)
Genomes Max Group AF 0.20647481 (EAS)
Exomes Max Group AF 0.2110853 (EAS)
ClinVar RCV:
RCV001516007
ClinVar Variation:
1167092
dbSNP:
3731055
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14178939C>T , CM000665.2:g.14178939C>T GRCh38
NC_000003.11:g.14220439C>T , CM000665.1:g.14220439C>T GRCh37
NC_000003.10:g.14195443C>T NCBI36
NG_011763.1:g.4734G>A , LRG_472:g.4734G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000306024.4:c.21+58C>T MANE Select ENSP00000302160.3:n.21+58C>T
ENST00000306024.3:c.21+58C>T ENSP00000302160.3:n.21+58C>T
NM_014463.2:c.21+58C>T NP_055278.1:n.21+58C>T
NM_014463.3:c.21+58C>T MANE Select NP_055278.1:n.21+58C>T
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