Canonical Allele Identifier: CA95700144
Gene: KLB HGNC NCBI

Linked Data

dbSNP Id: rs981102100
gnomAD v2: 4-39432134-C-T
gnomAD v3: 4-39430514-C-T
gnomAD v4: 4-39430514-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39430514C>T , CM000666.2:g.39430514C>T GRCh38
NC_000004.11:g.39432134C>T , CM000666.1:g.39432134C>T GRCh37
NC_000004.10:g.39108529C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000257408.5:c.826-3696C>T MANE Select ENSP00000257408.4:n.826-3696C>T
ENST00000257408.4:c.826-3696C>T ENSP00000257408.4:n.826-3696C>T
NM_175737.3:c.826-3696C>T NP_783864.1:n.826-3696C>T
XM_005262644.1:c.826-3696C>T XP_005262701.1:n.826-3696C>T
NM_175737.4:c.826-3696C>T MANE Select NP_783864.1:n.826-3696C>T