Canonical Allele Identifier: CA439948117

Gene: ALB

Linked Data

• gnomAD v4: 4-73413461-C-T
• MyVariant Identifiers: chr4:g.74279178C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413461C>T , CM000666.2:g.73413461C>T	GRCh38
NC_000004.11:g.74279178C>T , CM000666.1:g.74279178C>T	GRCh37
NC_000004.10:g.74498042C>T	NCBI36
NG_009291.1:g.14207C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.885C>T MANE Select	ENSP00000295897.4:p.Ile295=
ENST00000295897.8:c.885C>T	ENSP00000295897.4:p.Ile295=
ENST00000401494.7:c.540C>T	ENSP00000384695.3:p.Ile180=
ENST00000415165.6:c.309C>T	ENSP00000401820.2:p.Ile103=
ENST00000476441.6:c.*164C>T	ENSP00000423727.1:n.*164C>T
ENST00000484992.1:n.205C>T
ENST00000503124.5:c.435C>T	ENSP00000421027.1:p.Ile145=
ENST00000505649.5:n.571C>T
ENST00000509063.5:c.885C>T	ENSP00000422784.1:p.Ile295=
ENST00000511370.1:c.418C>T
ENST00000621085.4:c.491-1645C>T	ENSP00000483421.1:n.491-1645C>T
ENST00000621628.4:c.487-1641C>T	ENSP00000480485.1:n.487-1641C>T
NM_000477.5:c.885C>T	NP_000468.1:p.Ile295=
NM_000477.6:c.885C>T	NP_000468.1:p.Ile295=
NM_000477.7:c.885C>T MANE Select	NP_000468.1:p.Ile295=