Canonical Allele Identifier: CA99696193
Gene: ALB HGNC NCBI
MyVariant.info:
GRCh38 chr4:g.73404191C>T
GRCh37 chr4:g.74269908C>T
gnomAD v2:
4:74269908 C / T
gnomAD v3:
4:73404191 C / T
gnomAD v4:
chr4-73404191-C-T
Joint Max Group AF 0.00002253 (EAS)
Genomes Max Group AF 0.00015691 (EAS)
Exomes Max Group AF 0.00000105 (NFE)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404191C>T , CM000666.2:g.73404191C>T GRCh38
NC_000004.11:g.74269908C>T , CM000666.1:g.74269908C>T GRCh37
NC_000004.10:g.74488772C>T NCBI36
NG_009291.1:g.4937C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000441319.5:c.48-178C>T ENSP00000392541.1:n.48-178C>T
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