Canonical Allele Identifier: CA357247196

Gene: ALB

Linked Data

• dbSNP Id: rs199476397
• gnomAD v4: 4-73420278-C-T
• MyVariant Identifiers: chr4:g.74285995C>T (hg19) ; chr4:g.73420278C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420278C>T , CM000666.2:g.73420278C>T	GRCh38
NC_000004.11:g.74285995C>T , CM000666.1:g.74285995C>T	GRCh37
NC_000004.10:g.74504859C>T	NCBI36
NG_009291.1:g.21024C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1810C>T MANE Select	ENSP00000295897.4:p.Gln604Ter
ENST00000295897.8:c.1810C>T	ENSP00000295897.4:p.Gln604Ter
ENST00000401494.7:c.1465C>T	ENSP00000384695.3:p.Gln489Ter
ENST00000415165.6:c.1234C>T	ENSP00000401820.2:p.Gln412Ter
ENST00000476441.6:c.*1089C>T	ENSP00000423727.1:n.*1089C>T
ENST00000495173.1:n.118C>T
ENST00000503124.5:c.1360C>T	ENSP00000421027.1:p.Gln454Ter
ENST00000505649.5:n.1357C>T
ENST00000508932.5:n.200C>T
ENST00000509063.5:c.1785+639C>T	ENSP00000422784.1:n.1785+639C>T
ENST00000511370.1:c.1343C>T
ENST00000621085.4:c.1171C>T	ENSP00000483421.1:p.Gln391Ter
ENST00000621628.4:c.1171C>T	ENSP00000480485.1:p.Gln391Ter
NM_000477.5:c.1810C>T	NP_000468.1:p.Gln604Ter
NM_000477.6:c.1810C>T	NP_000468.1:p.Gln604Ter
NM_000477.7:c.1810C>T MANE Select	NP_000468.1:p.Gln604Ter