Canonical Allele Identifier: CA352748401
Gene: LAMB2 HGNC NCBI

Linked Data

dbSNP Id: rs1249885469
gnomAD v2: 3-49168565-G-C
gnomAD v4: 3-49131132-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49131132G>C , CM000665.2:g.49131132G>C GRCh38
NC_000003.11:g.49168565G>C , CM000665.1:g.49168565G>C GRCh37
NC_000003.10:g.49143569G>C NCBI36
NG_008094.1:g.7035C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000305544.9:c.733C>G MANE Select ENSP00000307156.4:p.Leu245Val
ENST00000305544.8:c.733C>G ENSP00000307156.4:p.Leu245Val
ENST00000418109.5:c.733C>G ENSP00000388325.1:p.Leu245Val
ENST00000494831.1:c.286C>G ENSP00000444751.1:p.Leu96Val
NM_002292.3:c.733C>G NP_002283.3:p.Leu245Val
XM_005265127.3:c.733C>G XP_005265184.1:p.Leu245Val
XM_005265127.4:c.733C>G XP_005265184.1:p.Leu245Val
NM_002292.4:c.733C>G MANE Select NP_002283.3:p.Leu245Val