Canonical Allele Identifier: CA2959239
Gene: ALB HGNC NCBI
MyVariant.info:
GRCh38 chr4:g.73404283T>C
GRCh37 chr4:g.74270000T>C
gnomAD v2:
4:74270000 T / C
gnomAD v3:
4:73404283 T / C
gnomAD v4:
chr4-73404283-T-C
Joint Max Group AF 0.00069448 (MID)
Genomes Max Group AF 0.00066403 (NFE)
Exomes Max Group AF 0.00073273 (MID)
ClinVar RCV:
RCV000312660
ClinVar Variation:
349615
dbSNP:
375806262
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404283T>C , CM000666.2:g.73404283T>C GRCh38
NC_000004.11:g.74270000T>C , CM000666.1:g.74270000T>C GRCh37
NC_000004.10:g.74488864T>C NCBI36
NG_009291.1:g.5029T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.8:c.-45T>C ENSP00000295897.4:n.-45T>C
ENST00000441319.5:c.48-86T>C ENSP00000392541.1:n.48-86T>C
ENST00000621628.4:c.-45T>C ENSP00000480485.1:n.-45T>C
NM_000477.5:c.-45T>C NP_000468.1:n.-45T>C
NM_000477.6:c.-45T>C NP_000468.1:n.-45T>C
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