Canonical Allele Identifier: CA439948416

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74283978T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418261T>C , CM000666.2:g.73418261T>C	GRCh38
NC_000004.11:g.74283978T>C , CM000666.1:g.74283978T>C	GRCh37
NC_000004.10:g.74502842T>C	NCBI36
NG_009291.1:g.19007T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1602T>C MANE Select	ENSP00000295897.4:p.His534=
ENST00000295897.8:c.1602T>C	ENSP00000295897.4:p.His534=
ENST00000401494.7:c.1257T>C	ENSP00000384695.3:p.His419=
ENST00000415165.6:c.1026T>C	ENSP00000401820.2:p.His342=
ENST00000476441.6:c.*881T>C	ENSP00000423727.1:n.*881T>C
ENST00000486939.1:n.256T>C
ENST00000503124.5:c.1152T>C	ENSP00000421027.1:p.His384=
ENST00000505649.5:n.1149T>C
ENST00000509063.5:c.1602T>C	ENSP00000422784.1:p.His534=
ENST00000511370.1:c.1135T>C
ENST00000621085.4:c.963T>C	ENSP00000483421.1:p.His321=
ENST00000621628.4:c.963T>C	ENSP00000480485.1:p.His321=
NM_000477.5:c.1602T>C	NP_000468.1:p.His534=
NM_000477.6:c.1602T>C	NP_000468.1:p.His534=
NM_000477.7:c.1602T>C MANE Select	NP_000468.1:p.His534=