Canonical Allele Identifier: CA357246106

Gene: ALB

Linked Data

• dbSNP Id: rs1421889284
• gnomAD v2: 4-74285246-C-T
• gnomAD v4: 4-73419529-C-T
• MyVariant Identifiers: chr4:g.74285246C>T (hg19) ; chr4:g.73419529C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419529C>T , CM000666.2:g.73419529C>T	GRCh38
NC_000004.11:g.74285246C>T , CM000666.1:g.74285246C>T	GRCh37
NC_000004.10:g.74504110C>T	NCBI36
NG_009291.1:g.20275C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1675C>T MANE Select	ENSP00000295897.4:p.His559Tyr
ENST00000295897.8:c.1675C>T	ENSP00000295897.4:p.His559Tyr
ENST00000401494.7:c.1330C>T	ENSP00000384695.3:p.His444Tyr
ENST00000415165.6:c.1099C>T	ENSP00000401820.2:p.His367Tyr
ENST00000476441.6:c.*954C>T	ENSP00000423727.1:n.*954C>T
ENST00000486939.1:n.329C>T
ENST00000503124.5:c.1225C>T	ENSP00000421027.1:p.His409Tyr
ENST00000505649.5:n.1222C>T
ENST00000508932.5:n.175+74C>T
ENST00000509063.5:c.1675C>T	ENSP00000422784.1:p.His559Tyr
ENST00000511370.1:c.1208C>T
ENST00000621085.4:c.1036C>T	ENSP00000483421.1:p.His346Tyr
ENST00000621628.4:c.1036C>T	ENSP00000480485.1:p.His346Tyr
NM_000477.5:c.1675C>T	NP_000468.1:p.His559Tyr
NM_000477.6:c.1675C>T	NP_000468.1:p.His559Tyr
NM_000477.7:c.1675C>T MANE Select	NP_000468.1:p.His559Tyr