Canonical Allele Identifier: CA439799212

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74274511A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408794A>C , CM000666.2:g.73408794A>C	GRCh38
NC_000004.11:g.74274511A>C , CM000666.1:g.74274511A>C	GRCh37
NC_000004.10:g.74493375A>C	NCBI36
NG_009291.1:g.9540A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.471A>C MANE Select	ENSP00000295897.4:p.Thr157=
ENST00000295897.8:c.471A>C	ENSP00000295897.4:p.Thr157=
ENST00000401494.7:c.138-561A>C	ENSP00000384695.3:n.138-561A>C
ENST00000415165.6:c.138-3202A>C	ENSP00000401820.2:n.138-3202A>C
ENST00000441319.5:c.477A>C	ENSP00000392541.1:p.Thr159=
ENST00000476441.6:c.80-561A>C	ENSP00000423727.1:n.80-561A>C
ENST00000503124.5:c.33-561A>C	ENSP00000421027.1:n.33-561A>C
ENST00000505649.5:n.157A>C
ENST00000509063.5:c.471A>C	ENSP00000422784.1:p.Thr157=
ENST00000510166.5:n.507A>C
ENST00000514786.1:n.440A>C
ENST00000515133.5:n.512A>C
ENST00000621085.4:c.471A>C	ENSP00000483421.1:p.Thr157=
ENST00000621628.4:c.471A>C	ENSP00000480485.1:p.Thr157=
NM_000477.5:c.471A>C	NP_000468.1:p.Thr157=
NM_000477.6:c.471A>C	NP_000468.1:p.Thr157=
NM_000477.7:c.471A>C MANE Select	NP_000468.1:p.Thr157=