Canonical Allele Identifier: CA95700195
Gene: KLB HGNC NCBI

Linked Data

dbSNP Id: rs576193353
gnomAD v2: 4-39432192-T-G
gnomAD v3: 4-39430572-T-G
gnomAD v4: 4-39430572-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39430572T>G , CM000666.2:g.39430572T>G GRCh38
NC_000004.11:g.39432192T>G , CM000666.1:g.39432192T>G GRCh37
NC_000004.10:g.39108587T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000257408.5:c.826-3638T>G MANE Select ENSP00000257408.4:n.826-3638T>G
ENST00000257408.4:c.826-3638T>G ENSP00000257408.4:n.826-3638T>G
NM_175737.3:c.826-3638T>G NP_783864.1:n.826-3638T>G
XM_005262644.1:c.826-3638T>G XP_005262701.1:n.826-3638T>G
NM_175737.4:c.826-3638T>G MANE Select NP_783864.1:n.826-3638T>G