Canonical Allele Identifier: CA127902
Gene: ALB HGNC NCBI

Linked Data

ClinVar Variation Id: 18197
ClinVar RCV Id: RCV000019842
dbSNP Id: rs77187142

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73415141G>C , CM000666.2:g.73415141G>C GRCh38
NC_000004.11:g.74280858G>C , CM000666.1:g.74280858G>C GRCh37
NC_000004.10:g.74499722G>C NCBI36
NG_009291.1:g.15887G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.1165G>C MANE Select ENSP00000295897.4:p.Asp389His
ENST00000295897.8:c.1165G>C ENSP00000295897.4:p.Asp389His
ENST00000401494.7:c.820G>C ENSP00000384695.3:p.Asp274His
ENST00000415165.6:c.589G>C ENSP00000401820.2:p.Asp197His
ENST00000476441.6:c.*444G>C ENSP00000423727.1:p.=
ENST00000484992.1:n.485G>C
ENST00000503124.5:c.715G>C ENSP00000421027.1:p.Asp239His
ENST00000504043.1:n.168G>C
ENST00000505649.5:n.851G>C
ENST00000509063.5:c.1165G>C ENSP00000422784.1:p.Asp389His
ENST00000511370.1:n.698G>C
ENST00000621085.4:c.526G>C ENSP00000483421.1:p.Asp176His
ENST00000621628.4:c.526G>C ENSP00000480485.1:p.Asp176His
NM_000477.5:c.1165G>C NP_000468.1:p.Asp389His
NM_000477.6:c.1165G>C NP_000468.1:p.Asp389His
NM_000477.7:c.1165G>C MANE Select NP_000468.1:p.Asp389His