Canonical Allele Identifier: CA357234601

Gene: ALB

Linked Data

• dbSNP Id: rs1332629192
• gnomAD v4: 4-73404374-C-T
• MyVariant Identifiers: chr4:g.74270091C>T (hg19) ; chr4:g.73404374C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404374C>T , CM000666.2:g.73404374C>T	GRCh38
NC_000004.11:g.74270091C>T , CM000666.1:g.74270091C>T	GRCh37
NC_000004.10:g.74488955C>T	NCBI36
NG_009291.1:g.5120C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.47C>T MANE Select	ENSP00000295897.4:p.Ala16Val
ENST00000295897.8:c.47C>T	ENSP00000295897.4:p.Ala16Val
ENST00000401494.7:c.47C>T	ENSP00000384695.3:p.Ala16Val
ENST00000415165.6:c.47C>T	ENSP00000401820.2:p.Ala16Val
ENST00000441319.5:c.53C>T	ENSP00000392541.1:p.Ala18Val
ENST00000476441.6:c.47C>T	ENSP00000423727.1:p.Ala16Val
ENST00000503124.5:c.-134C>T	ENSP00000421027.1:n.-134C>T
ENST00000509063.5:c.47C>T	ENSP00000422784.1:p.Ala16Val
ENST00000510166.5:n.88C>T
ENST00000514786.1:n.48+38C>T
ENST00000515133.5:n.88C>T
ENST00000621085.4:c.47C>T	ENSP00000483421.1:p.Ala16Val
ENST00000621628.4:c.47C>T	ENSP00000480485.1:p.Ala16Val
NM_000477.5:c.47C>T	NP_000468.1:p.Ala16Val
NM_000477.6:c.47C>T	NP_000468.1:p.Ala16Val
NM_000477.7:c.47C>T MANE Select	NP_000468.1:p.Ala16Val